Clinical Research Coordinator- Mt Lebanon, PA

Preferred Primary Care Physicians, Inc.•Pittsburgh, PA

About The Position

Preferred Primary Care Physicians, one of Pittsburgh's largest private physician practices, is looking for a full-time Clinical Research Coordinator. The clinical research coordinator will be responsible for assisting with daily clinical research operations, implementation and conduct of multiple clinical trials and ensuring all research activities are coordinated in compliance with federal, state and local regulations. Excellent verbal and written communication skills and an ability to communicate with a diverse group of people in a clear and concise manner. Detail oriented and highly organized. Self-motivated with the ability to work effectively while managing multiple studies and projects. Promote a team approach with high standards of professionalism and productivity. Expected Routine Responsibilities Day to day clinical research and operational oversight of the research office and the coordination with the physician's clinical office, in accordance with GCP guidelines and all federal, state and local regulations. Exhibits strong study management skills through organization, communication, problem solving, conflict resolution and leadership.. Recruits and screens potential study participants and performs intake assessments Creates and/or maintains all documents and records related to the study Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress Manages the inventory of equipment and supplies related to the study and orders more as needed Collects specimens and inputs data and patient information into electronic systems Creates reports on each study, including notes on protocols, workload, data collection, and more

Requirements

Excellent written and verbal communication skills
Superior organizational and time management skills
Capable of working independently with minimal supervision and also as part of a team
Skilled with standard computer programs including the MS Office suite
Understanding of medical terminology as well as standard clinical procedures and protocols
High School Diploma or GED required.
Minimum two (2) years of clinical research experience, or equivalent experience in a health-related field (e.g., RN, LPN, MA), or equivalent combination of education and experience.
Ability to establish and maintain effective working relationships.
Ability to react calmly in emergency situations.
Ability to communicate clearly.
Ability to read, understand and respond to detailed written and oral instructions.
Ability to be self-motivated, work independently, and multi-task.

Nice To Haves

Candidates with at least a two (2) year degree highly preferred.

Responsibilities

Day to day clinical research and operational oversight of the research office and the coordination with the physician's clinical office, in accordance with GCP guidelines and all federal, state and local regulations.
Exhibits strong study management skills through organization, communication, problem solving, conflict resolution and leadership.
Recruits and screens potential study participants and performs intake assessments
Creates and/or maintains all documents and records related to the study
Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
Manages the inventory of equipment and supplies related to the study and orders more as needed
Collects specimens and inputs data and patient information into electronic systems
Creates reports on each study, including notes on protocols, workload, data collection, and more